Clinical Data Associate
AI summary
Divine AG Solutions Limited is hiring a Clinical Data Associate to manage clinical trial data quality, EDC systems, and data-related documentation. The full-time remote role requires at least 4 years of data coordination or management experience in a pharmaceutical, biotech, or contract research organization setting.
- Full-time remote clinical data role in Nigeria
- Requires 4 years of data coordination or management experience
- Involves EDC systems, data validation, and query management
- Requires experience with Medidata Rave or Oracle Inform
- Reports to the Clinical Data Management department
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- Required4+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in associate, data specialist, remote workerThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Clinical Data Associate evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Divine AG Solutions Limited and the role in Not specified.
- Add concrete examples related to associate, data specialist, remote worker, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from MyJobMag Nigeria; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- MyJobMag Nigeria
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Clinical Data Associate role in associate, data specialist?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Divine AG Solutions Limited before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
Divine AG Solutions Limited (RC 1243335) was incorporated in 2015 to provide recruitment and outsourcing services in accordance with the terms agreed between us and our clients. Our goal is to meet the needs of our clients ranging from individual clients, government parastatals, corporate organizations, manufacturing companies, public sectors/organizations, ... Clinical Data Associate Job Type Full Time , Remote Qualification BA/BSc/HND Experience: 4 years Location Nigeria Job Field Data, Business Analysis and AI Position Summary The position is responsible for coordinating activities associated with the data management process throughout a clinical trial and the overall quality and integrity of data input and output. This position reports to management within the Data Management department. Essential Functions Independently reviews clinical study data entered in the EDC systems, generates queries as needed and works with site data entry staff and site Clinical Research Associates (CRAs) to ensure that data collected is accurately reported. Drafts data-related manuals and plans, including but not limited to the Data Management Plan (DMP), eCRF Completion Guidelines (CCGs), Database Specification, and Data Validation Specification (DVS). Submits near-final manuals and plans to the Clinical Data Manager (CDM) for limited final review and approval. Performs database User Acceptance Testing, including high-level script writing and execution. Maintains and tracks monthly clinical research project data metrics. Reviews metrics to assist the CDM in analyzing, identifying and reporting data and trends. Works with the CDM on data coding and maintaining appropriate WHODrug and MedDRA licenses. Works with the CDM on data reconciliation, including serious adverse events (SAE) and external lab data reconciliation. Performs database user administration tasks including granting, modifying, and revoking access rights. Performs bi-annual reviews of database users in collaboration with NK Clinical Project Managers. Represents the Clinical Data Management department in Sponsor meetings, audits and project team meetings. Maintains established timelines for assigned projects. Works extensively with project leaders, clinical team members and Sponsors in managing their clinical data needs. Encourages collaborations and builds working relationships with functional groups that are contributing to the project plan. Liaises with clinical, safety and regulatory organizations for coordination of clinical trial activities. Writes controlled documents and department training modules related to the Data Management function for review and approval by management. Participates in training clinical team members. Performs other related duties as assigned. Job Requirements: Associate's Degree with preference to degrees in a health science, statistics, or data management field. Must have at least 4 years of data coordination or data management experience: in a biotechnology/pharmaceutical, academic or contract research organization setting. Required specialized/technical skills include: Experience: with clinical data management, clinical study database design and implementation and generation of data reports and listings Experience: with hands-on management and testing of clinical databases Experience: utilizing programs to code medical terms and medications Experience: with commercial electronic data capture systems (EDC) such as Medidata Rave and Oracle Inform Strong computer skills with proficiency in Microsoft Office applications Possess strategic thinking, contingency planning and problem-solving skills Strong interpersonal and communication skills, both oral and written Ability to work collaboratively with cross-functional teams Excellent planning and organizational skills Strong knowledge of the clinical drug development process Demonstrated skill with establishing and documenting standard processes by which project tracking data is collected, updated and reported to the project team Check how your CV aligns with this job Method of Application Interested and qualified candidates should forward their CV to: divineagsolutionsltd@gmail.com using the Job Title as the subject of the email. Build your CV for free. Download in different templates.